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Clinical Trials/NL-OMON19993
NL-OMON19993
Completed
Not Applicable

High-Flow Nasal Cannula for severe COVID-19, a multicentre prospective cohort study

o sponsors0 sites600 target enrollmentTBD
Conditions<p>COVID-19</p>

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
<p>COVID-19</p>
Sponsor
o sponsors
Enrollment
600
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
o sponsors

Eligibility Criteria

Inclusion Criteria

  • The population included will be hospitalized patients with confirmed COVID\-19, \= 18 years old with isolated severe hypoxic respiratory failure defined as: SpO2 \< 92% and/or BF\>30/min despite treatment with at least 6 L/min oxygen therapy on nasal cannula. These patients may be included at the pulmonary departments delivering COVID\-19 care, intensive care units or directly on the Emergency department. SARS\-CoV\-2 negative patients (nasopharyngeal PCR) will be excluded for this analysis, retrospectively.
  • Inclusion criteria
  • In order to be eligible to participate in this study, a subject must meet all of the following inclusion criteria:
  • ? Age \= 18 years
  • ? Admitted to the hospital
  • ? Suspect of COVID\-19 or nasopharyngeal swab PCR confirmed COVID\-19
  • ? SpO2 \< 92% and/ or breathing frequency \>30/min despite at least 6L O2/min on nasal cannula.

Exclusion Criteria

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • ? Reasons for direct intubation, as per local standard of clinical care.
  • ? Patient does not accept treatment with HFNC
  • ? Anatomic abnormalities (recent surgery of the face, nose, or airway) that preclude an appropriate\-fitting nasal cannula

Outcomes

Primary Outcomes

Not specified

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